Musculoskeletal Flashcards

1
Q

What is the majority of disease risk determined by in Ankylosing spondylitis

A

90% have HLA-B27

Male predominated

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2
Q

Describe the typical disease course for Ankylosing spondylitis

A

Before 30 years old

Insidious onset of lower back pain with spinal morning stiffness relieved by exercise

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3
Q

What are the 3 articular features of Ankylosing spondylitis

A

Inflammatory back pain:
Patients usually have morning stiffness and pain that starts in the sacroiliac joints and radiates to the buttocks. There is often tenderness of the sacroiliac joints. Advanced diseases sees the loss of lumbar lordosis and exaggeration of thoracic kyphosis with the neck stooped forward (Question mark posture).

Peripheral enthesitis:
Achilles tendonitis, Plantar fasciitis and tibial tuberosity. Painful in the morning - potential swelling

Peripheral arthritis:
Asymmetric joint involvement including - Hips, Shoulder, Chest wall, Pubic symphysis

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4
Q

What are the extra-articular features of Ankylosing spondylitis

A

Eyes - Acute anterior uveitis
CV - Aortitis to AR, Fibrosis to AV Block
Resp - Limited chest expansion to Restrictive, Fibrosis of upper lobes
Renal - IgA nephropathy
Neuro - 2o to fractures of fused spine - Cauda equina
Met - Osteopenia/Osteoporosis

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5
Q

What are the investigative results in Ankylosing spondylitis

A

Potential normocytic anaemia - FBC
Inflammatory markers may be elevated - ESR, CRP
Sacroiliitis or enthesitis/Spinal Osteopenia - XR
MRI - More sensitive
DEXA - Osteoporosis

Seronegative - -ve Rheuamtoid factor and ANA

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6
Q

What is Gout

A

Gout is a crystal arthropathy.

This is arthritis due to monosodium urate (MSU) crystal deposition within joints causing acute inflammation and tissue damage. These deposits are called Tophi

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7
Q

What joints are usually affected in Gout

A

Most of the time it is the MTP joint of the big toe (podagra)

Other joints:
Ankle,
Foot,
Small joints in hands,
Wrist, 
Elbow,
Knee

Potential to be polyarticular but is usually mono

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8
Q

What is the primary cause of Gout and what are the precipitating factors to this

A

The primary cause if hyperuricaemia usually due to inadequate excretion of uric acid from purine nucleotides

RFs: MALE
Dietary: Meat, Seafood, Alcohol, High triglycerides
Drug: Diuretics, Chemotherapy
Medical: Obesity, CHD, CKD, DM, HF, HTNm Psoriasis

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9
Q

What are long term complications of Gout

A

Urate deposits - Tophi

Renal disease - Stones, interstitial nephritis

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10
Q

What are the signs and symptoms of Gout

A

Swollen, tender, red joints - Peaks within 24hrs. Attack resolves in 5-15 days untreated.

Potential - Tenosynovitis, bursitis and cellulitis

Chronic tophaceous gout - Large deposits around extensors and ears

Crepitus and deformity

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11
Q

What are the investigative findings in gout

A

Negatively birefringent urate needle-shaped crystals and increased WCC - Polarised light microscopy of synovial fluid

High serum urate

Junta-Articular erosions - XR

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12
Q

What is Pseudo-gout

A

This calcium pyrophosphate deposition rather than monosodium urate and usually affecting larger joints

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13
Q

What is the presentation of Pseudo-gout

A

Acute monoarticular or oligoarticular arthritis.

Usually affects the knees

Often also wrists, shoulders, ankles, hands and feet. Almost any joint may be affected.

Presentation is similar (but usually milder) to acute gout, with acute joint pain and swelling.

Affected joints are acutely inflamed with swelling, effusion, warmth, tenderness and pain on movement.

Attacks may be associated with fever and raised white cell count.

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14
Q

What are the investigative findings in Pseudo-gout

A

Positive intracellular or extracellular birefringent rhomboid-shaped crystals - Polarised light microscopy of synovial fluid

Soft tissue calcium deposition - XR

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15
Q

What are the risk factors and associations of Fibromyalgia

A
RFs
Female
Middle age
Low household income
Divorced
Low educational status

Chronic fatigue syndrome
IBS
Chronic headache syndrome

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16
Q

What are the main signs and symptoms of Fibromyalgia

A

Pain - Chronic (>3months) and widespread (Left and right, above and below diaphragm)

Fatigue - Profound with unrefreshing sleep and significant fatigue and pain with small increases in exertion.

Widespread and severe tender points

Other features:
Morning stiffness
Paraesthesiae
Headaches
Low mood
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17
Q

What are investigations in Fibromyalgia geared towards

A
Exclusion of
Rheumatoid arthritis
Polymyalgia rheumatica
Vasculitis
Hyothyroidism
Myeloma
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18
Q

Who usually gets Giant cell arteritis

A

Temporal arteritis:
Woman older than 50
If they are younger then consider Takayasu’s.

It is associated with Polymyalgia rheumatica

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19
Q

What are the signs and symptoms of Giant cell arteritis

A

Headache
Temporal artery and scalp tenderness
Loss of vision

Malaise
Dyspnoea
Weight loss
Morning stiffness

Risk of irreversible bilateral vision loss

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20
Q

What are the normal investigative results in Giant cell arteritis

A
Increased ESR and CRP
Thrombophilia
Increased ALP
Anaemia
Biopsy within 14 days of starting steroids - Beware of skip lesions
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21
Q

How is Giant cell arteritis treated

A

No visual symptoms - Oral Prednisolone

Visual symptoms - IV MethylPrednisolone

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22
Q

What are the symptoms of localised and generalised Osteoarthritis

A

Localised disease:
Hx Physically active
Pain and crepitus on movement
Pain is worse with prolonged activity.

Morning stiffness lasting under 30 minutes. (Longer than this may be suggestive of RA)

Joint instability can lead to perceived lack of power

Generalised disease:
Joint tenderness
Derangement and bony swelling (Heberden’s at DIP, Bouchard’s at PIP)
Reduced range of movement

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23
Q

Which joints are usually affected in localised and generalised Osteoarthritis

A

Localised:
Knee or Hip

Generalised:
DIP, PIP, CMC joints

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24
Q

What are the investigative findings in Osteoarthritis

A
Plain XR
Loss of joint space
Osteophytes
Subarticular sclerosis
Subchondral cysts

Potentially elevated CRP

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25
Q

What are the risk factors for Carpal tunnel syndrome

A

Women

Genetic:
Short stature
Fix
Hereditary neuropathy

2o:
Obesity
Colles fracture
Trauma to wrist
SOL in wrist
DM
Hyperthyroidism
Menopause
Inflammatory arthritides 
Acromegaly
Renal dialysis
Amyloidosis

Pregnancy

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26
Q

What are the characteristic features of Carpal tunnel syndrome

A

Aching pain in the hand and arms (especially at night), and paraesthesiae in thumb, index, and middle fingers: relieved by dangling the hand over
the edge of the bed and shaking it (remember ‘wake and shake’).

There may be sensory loss and weakness of abductor pollicis brevis ± wasting of the thenar eminence. Light touch, 2-point discrimination, and sweating may be impaired.

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27
Q

What are the investigative findings in Carpal tunnel syndrome

A

Tinnel’s - Tapping lightly over the median nerve at the wrist causes a distal paraesthesia in the median nerve distribution.
Phalens - Flexing the wrist for 60 seconds causes pain or paraesthesia in the median nerve distribution.

ENG - The median nerve is stimulated proximal to the carpal ligament and compound muscle action potential is picked up over the thenar eminence.
EMG - Useful but ENG better
US - Confirming

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28
Q

What is Systemic sclerosis

A

A multisystem autoimmune disease characterised by functional and structural abnormalities of small blood vessel, fibrosis of skin and internal organs, and production of auto-antibodies

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29
Q

What are the antibodies involved in Systemic sclerosis

A

90% of cases are ANA positive
30-40% have anticentromere antibodies

Limited: 70-80% Anticentromere antibodies

Diffuse: 40% Antitopoisomerase-1
20% anti-RNA polymerase

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30
Q

What are the 2 main types of Systemic sclerosis and the main features of both

A
Diffuse Cutaneous Systemic Sclerosis (40%)
Raynaud's phenomenon
Followed by skin changes with truncal involvement
Tendon friction
Joint contracture
Early lung disease
Heart, GI and renal disease
Nail-­‐fold capillary dilatation
Limited Cutaneous Systemic Sclerosis (60%)
CREST Syndrome
Calcinosis
Raynaud's phenomenon
(O)esophageal dysmotility
Sclerodactyly
Telangiectasia
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31
Q

What are the signs and symptoms of Systemic sclerosis separated by system

A

Skin - Raynaud’s disease

Hands - Initially swollen and painful then later they thicken and tighten and become shiny. Changes in pigmentation and Finger ulcers

Face - Microstomia - Puckering of skin around mouth. Telangiectasia

Lungs - Fibrosis to hypertension

Heart - Pericarditis or effusion, fibrosis, HF

GI - Dry mouth, oesophageal dysmotility, GORD, Gastric paresis

Kidneys - Hypertensive renal crisis, Chronic renal failure

Neuromuscular - Trigeminal neuralgia, wasting and weakness

Others - Hypothyroidism, impotence

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32
Q

Aside from the 1st line investigation of Systemic Sclerosis what other investigations can supplement the finding of ANA antibodies

A
Lungs - CXR, PFTs, CT
Heart - ECG, Echo
GI - Endoscopy, Barium studies
Kidneys - U&Es, creatinine clearance
Neuromuscular - EMG, biopsy
Joints - Radiography
33
Q

What is Systemic lupus erythematosus (SLE)

A

This is a multi-system inflammatory autoimmune disorder associated with tissue damage caused by vascular immune complex deposition

34
Q

What are the presentations of SLE

A
General: 
Fever
Fatigue
Weight loss
Lymphadenopathy
Splenomegaly

Raynaud’s
Oral ulcers
Skin rash - Malar/Discoid + Photosensitivity

Systemic:
MSK - Arthritis, tendonitis, myopathy
Heart - Pericarditis, arrhythmias, Libman-Sacks endocarditis
Lung - Pleurisy, effusion, atelectasis
Neurological - Headache, stroke, cranial nerve palsies
Psychiatric - Depression, psychosis
Renal - Glomerulonephritis

35
Q

What are the diagnostic criteria for SLE

A

SLE is an appropriate diagnosis when 4 or more criteria (at least 1 clinical and 1 lab) are met or biopsy-proven lupus nephritis with positive AN and anti-DNA

Clinical:
Acute cutaneous lupus
Chronic cutaneous lupus
Non scarring alopecia
Oral/nasal ulcers
Synovitis
Serositis - Lung or Pericardial
Urinanalysis - Proteinuria or red cell casts 
Neurological features
Haemolytic anaemia
Leucopenia
Thrombocytopenia
Lab criteria
ANA +ve 95%
Anti-dsDNA
Anti-Smith Abs
Antiphospholipid Abs
Low complement
\+ve Direct Coombs test
36
Q

What is Cervical spondylosis

A

Progressive degenerative process affecting the cervical vertebral bodies and intervertebral discs, and causing compression of the spinal cord and/or nerve roots

37
Q

What are the common presentations of Cervical spondylosis

A

Neck:
Neck stiffness

Pain:
Arm (Stabbing or dull)
Face
Breast
Chest

Legs:
Weak and stiff legs
Gait disturbances

General:
Paraesthesia
Weakness
Clumsiness

38
Q

What are the signs of Cervical spondylosis

A
Arms: 
Atrophy of the forearm and hand muscles
Segmental muscle weakness in a nerve root distribution
Hyporeflexia
Sensory loss
Pseudoathetosis
Legs - In cord compression
Increased tone
Weakness
Hyper-reflexia
Babinski +ve
Reduced vibration and proprioception
39
Q

What are the main investigations used in Cervical spondylosis

A

Cervical MRI - Bone destruction, Cord/ Nerve compression

Cervical XR - Degenerative joint, degenerative disc, fracture

40
Q

What is Sjögren’s syndrome

A

A chronic systemic inflammatory autoimmune disorder characterised by lymphatic infiltration into exocrine glands especially the lacrimal gland and salivary glands

41
Q

What are the classifications for Sjögren’s syndrome

A

It can be primary occurring alone or secondary occurring with another autoimmune inflammatory disease such as Rheumatoid arthritis, SLE or Systemic sclerosis (Scleroderma)

42
Q

What are the main features of Sjögren’s syndrome

A

Dry eyes
Dry mouth
Parotid swelling

Dry URT - Dry cough
Dry skin on hair
Dry vagina
Reduced GI mucus secretions - Reflux oesophagitis, gastritis, constipation
General: Depression, weight loss, fever, fatigue

43
Q

What are the main investigations for Sjögren’s syndrome

A

Schrimer’s test - A filter paper is placed in the lower conjunctival sac. The test is positive if less than 5 mm of paper is wetted after 5 minutes.

Antibodies - Antibodies to the ribonucleoproteins 60 kD Ro and La are found in up to 90% of patients with Sjogren syndrome.

Fluorescein/Rose Bengal Stains
May show punctate or filamentary keratitis

Other Investigations
Reduced parotid salivary flow rate
Reduced uptake or clearance on isotope scan

Biopsy of salivary or labial glands

44
Q

What is Septic arthritis

A

This is defined as infection of 1 or more joints caused by pathogenic inoculation of microbes.

45
Q

What are risk factors for Septic arthritis

A
Increased age >80
DM
Prior joint damage
Joint surgery
Prosthetic joints
Skin infection in combination with joint prosthesis
Immunodeficiency
46
Q

What are the presenting symptoms and signs of Septic arthritis

A

Hot, Swollen, Painful joint(s) + Restriction of movement
Fever + Rigors

Knee most common site of infection

47
Q

What are the main investigations necessary in Septic arthritis

A

Joint aspiration
Blood cultures prior to antibiotics
CRP/ESR/WCC - Elevated but not diagnostic

48
Q

What are the important characteristics of Rheumatoid arthritis

A

It is a chronic systemic inflammatory disease

Symmetrical, deforming, peripheral polyarthritis

Increases risk of CVD (Maybe attributed to higher incidence in smokers) and is associated with HLA-DR1 & DR4

Potential extra-articular features

49
Q

What are the typical and less typical presentations of Rheumatoid arthritis

A

Typical: Symmetrical swollen, painful, stiff small joints of hands and feet - Worse in the morning. Fluctuate and large joints may become involved.

Possible presentations (No need to learn):
Sudden onset widespread arthritis
Recurring arthritis of various joints
Persistent monoarthritis
Systemic illness with extra-articular symptoms - Fatigue, fever, weight loss, pericarditis, pleurisy
Polymyalgic onset - Vague limb girdle aches
Reccurent soft tissue problems

50
Q

What are the early and late signs of Rheumatoid arthritis

A

Early (Inflammation no damage):
Swollen - MCP, PIP, Wrist or MTP joints.
Reduction in range of motion
Tenderness

Later (Joint damage, and deformity):
Ulnar deviation and subluxation of the wrist and fingers
Boutonniere and swan-neck deformities of fingers or z-deformity of thumbs occur.
Hand extensor tendons may rupture.
Wasting of small hand muscles
Palmar erythema
Rheumatoid nodules - firm subcutaneous nodules
Elbows, ulnar margin, palms and over extensor tendons

51
Q

What are the main investigations need for Rheumatoid arthritis

A

Rheumatoid factor 60-70%
XR - Deformity, Osteopaenia, Narrowing of joint space, Soft tissue swelling
Anaemia of chronic disease
ESR/CRP/Platelet - Elevated

52
Q

What is Reactive arthritis

A

This is a sterile arthritis that occurs after an infection elsewhere in the body (GI or UG)

53
Q

Who is usually affected by Reactive arthritis

A

Young men (20x more common)

HLA-B27 associatino

GI - Salmonella, shigella, yersinia, campylobacter
UG - Chlamydia

54
Q

What are the signs and symptoms of Reactive arthritis

A

Arthritis - Asymmetrical oligoarthritis - lower extremities - Sausage-shaped digits

Conjunctivitis

Urethritis - Burning or stinging when passing urine

Sacroiliitis - Lower back pain

Enthesitis - Painful heel

Oral ulceration
Circinate balanitis
Keratoderma Blennorrhagica
Nail dystrophy
Hyperkeratosis
Onycholysis

Reiter’s Triad: Conjunctivitis, urethritis, and arthritis

55
Q

What are the investigative findings in Reactive arthritis

A

ESR/CRP - Elevated
XR - Sacroiliitis and enthesitis
HLA-B27

56
Q

What is Osteomyelitis

A

Infection of the bone leading to inflammation, necrosis and new bone formation

Staph A
Group A Strep

57
Q

Who is affected by Osteomyelitis

A

Young children
Trauma
Operative
Ulcers

DM
Immunosuppression
IVD
Prosthesis
Sickle-cell anaemia
58
Q

What are the signs and symptoms of Osteomyelitis

A
Pain
Fever + Rigors, Malaise
Erythema
Tenderness
Swelling 
Warmth
Limited movement
Seropurulent discharge
59
Q

What are the investigative findings in Osteomyelitis

A

ESR/CRP/WCC - Raised

XR - Acute disease - Osteopenia appears 6-7 days after infection onset

60
Q

What is Polymyalgia rheumatica

A

Inflammatory condition characterised by severe bilateral pain and morning stiffness of the shoulder, neck and pelvic girdle.

Associated with GCA

61
Q

What are the common signs and symptoms of Polymyalgia rheumatica

A

Limb girdle stiffness and pain
Morning stiffness of greater than 45 minutes
Symptoms worse when waking
Low-grade fever + other flu like features

62
Q

What are the appropriate investigations for Polymyalgia rheumatica

A

ESR/CRP - Elevated

US - Bursitis/Joint effusion

63
Q

What is the treatment of Polymyalgia rheumatica

A

Coricosteriods - Oral Prednisolone 15mg/day generally response should be very quick

Monitor for adverse effects of steroids

Methotrexate may be considered for patients with prolonged therapy

64
Q

What are Idiopathic inflammatory myopathies

A

A heterogenous group of skeletal muscle that have in common - Proximal muscle weakness and inflammation on muscle biopsy

Polymyositis
Dermatomyositis

65
Q

What are causes of the Idiopathic inflammatory myopathies

A

They are both autoimmune diseases with viral infection being implicated

66
Q

Who is usually affected by the Idiopathic inflammatory myopathies

A

Polymyositis - 30-60
Dermatomyositis - Any age (Biphasic)

Both are more common in women

67
Q

What are the signs and symptoms of Polymyositis

A

Bilateral proximal muscle weakness, wasting and myalgia

If the muscles of the pharynx or oesophagus are involved then this can lead to dysphonia and dysphagia

68
Q

What are the signs and symptoms of Dermatomyositis

A

Bilateral proximal muscle weakness, wasting and myalgia

If the muscles of the pharynx or oesophagus are involved then this can lead to dysphonia and dysphagia

Rash:

  • Purplish rash on upper eyelid with oedema (Heliotrope)
  • Rash around the whole upper girdle (Shawl rash)
  • Facial rash
  • Gottron’s papules (Red scaly rash on knuckles and elbows)
  • Nail fold changes
69
Q

How is Polymyositis diagnosed

A

Definitive diagnosis: Muscle Biopsy - Endomysial inflammatory infiltrates, Muscle necrosis, atrophy, muscle fibre regeneration

Creatine kinase - Up to 50x normal
EMG - Reduced activity
Antibodies: ANA, Anti-Mi-2, Anti-SRP, Anti-Jo-1
Myoglobin - Useful for disease severity
Enzymes less specific than CK: Aldolase, LDH, ALT

70
Q

How is Dermatomyositis diagnosed

A

Definitive diagnosis: Muscle Biopsy - Perifascicular atrophy, Perivascular/Perimysial inflammation

Creatine Kinase - Not as useful in Poly
EMG - Reduced activity
Antibodies: ANA, Anti-Mi-2, Anti-Jo-1
HLA-DR3/5 Association
Myoglobin - Useful for disease severity

Enzymes less specific than CK: Aldolase, LDH, ALT

71
Q

What are Vasculitides

A

These are inflammatory disorders of blood vessels

It may be primary or secondary to another disease: SLE, RA, HEPB/C, HIV.

72
Q

How are Vasculitides classed?

A

By the type of vessel they affect
Large: Giant cell arteritis, Takayasu’s arteritis
Medium: Polyarteritis nodosa
Small: Microscopic polyangiitis, Eosinophilic granulomatosis with polyangiitis (Churg Strauss Syndrome), Granulomatosis with polyangiitis (Wegener’s Granulomatosis),

All: Behçet’s disease

73
Q

Outline Takayasu’s arteritis

A

What: Aorta and it’s major branches

Epi: Young women (Asian)

Signs and symptoms:

  • Turbulent blood flow leading to bruits (Potentially in all major arteries)
  • Blood pressure asymmetry
  • Reduced or absent peripheral pulses
  • Limb claudication
  • FLAWS

Diagnosis:
- CT Angio/MRA showing skip lesions

74
Q

Outline Polyarteritis nodosa

A

What: Skin, Renal and mesenteric

Epi: Hep B individuals - Rosary sign on renal angiogram

Signs and symptoms:

  • Joint & Muscle pain
  • Skin rash - Livedo reticularis
  • Palpable purpura
  • Peripheral neuropathy
  • GI bleeding
  • Renal failure
  • HTN + MI

Diagnosis:

  • Angiography - Cluster or small aneurysms
  • Biopsy (Skin, Blood vessels, nerve, muscles…)
75
Q

Outline Microscopic polyangiitis

A

What: Non-granulamatous inflammation in blood vessel of: Eyes, Larynx, Lungs and Kidneys

Epi: Middle Ages

Signs and symptoms:
Similar signs and symptoms to Wegener’s but more of the glomerulonephritis aspects

Diagnosis:

  • pANCA
  • Biopsy of affected organ (Skin, Kidney or Lung)
76
Q

Outline Eosinophilic granulomatosis with polyangiitis (Churg Strauss Syndrome)

A

What: Granulamatous inflammation with Eosinophilia in blood vessel of: Eyes, Larynx, Lungs and Kidneys

Epi: Hx Atopy

Signs and symptoms:
Similar signs and symptoms to Wegener's but with Allergic symptoms beforehand
- Asthma
- Chronic rhinosinusitis
- Blood Eosinophilia
- Peripheral neuropathy

Diagnosis:

  • pANCA
  • ECG
  • Echo
77
Q

Outline Granulomatosis with polyangiitis (Wegener’s Granulomatosis)

A

What: Granulamatous inflammation in blood vessel of: Eyes, Ears, Nose, Larynx, Lungs and Kidneys

Epi: White

Signs and symptoms:

  • Eyes - Painful exophthalmos, Diplopia, Optic nerve ischaemia, Sceritis or Uveitis
  • Ear - Otitis, Deafness
  • Nose - Saddle nose deformity, Recurrent sinusitis
  • Larynx - Hoarse voice, Collapse
  • Lung - Nodules (Biopsied)
  • Renal - Glomerulonephritis, KF

Diagnosis:

  • cANCA
  • Biopsy of affected organ (Skin, Kidney or Lung)
78
Q

Outline Behçet’s disease

A

What: Affects all vessels

Epi: Greek, Turkish, HLA-

Signs and symptoms:

  • Recurrent oral ulcers (Larger, more painful, and longer to heal than Aphthous ulcers) - Almost continuously present
  • Genital ulcers
  • Anterior Uveitis - Sterile pus (Hypopyon), Painful, Redness
  • Posterior Uveitis - Painless, floaters, decreased vision
  • Folliculitis
  • Erythema nodosum
  • Arthritis
  • Colitis

Diagnosis:

  • Clinical based on symptoms
  • Pathergy test - Pin prick becomes an ulcer after 2 days